US3937704A - 3-(methylsulfinyl)cinnolinones and their derivatives - Google Patents

3-(methylsulfinyl)cinnolinones and their derivatives Download PDF

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US3937704A
US3937704A US05/416,332 US41633273A US3937704A US 3937704 A US3937704 A US 3937704A US 41633273 A US41633273 A US 41633273A US 3937704 A US3937704 A US 3937704A
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methylsulfinyl
solution
methyl
cinnolinone
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Maximilian von Strandtmann
John Shavel, Jr.
Sylvester Klutchko
Marvin Cohen
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Warner Lambert Co LLC
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/28—Cinnolines

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  • the present invention relates to 3-substituted cinnolinones having the following structural formula: ##SPC3##
  • R 1 is H, lower alkyl, aralkyl or acyl and R 2 and R 3 are hydrogen, halogen, lower alkoxy or lower alkyl, and X is ##EQU2## ##SPC4## and CH 3 COOCH 2 S--.
  • lower alkyl and the “alkyl” portion of lower alkoxy is meant to contain from 1 to 6 carbon atoms such as methyl, ethyl, propyl, isopropyl and the like.
  • aralkyl is meant to be those groups such as phenyl lower alkyl, typically benzyl, phenethyl and the like.
  • acyl includes lower alkanoic acids from 1 to 6 carbons, typically acetic, propionic, and the like.
  • the compounds of this invention exhibit potent immuno-suppressant activity in a mammalian host.
  • they when they are tested in accordance with the procedure described by Jerne, et al., in "Cell-Bound Antibodies," Page 109, Wistar Institute Press, Philadelphia, Pennsylvania (1963), they are capable of inhibiting 90% of the antibody formation at a dose level of 100 mg/kg intraperitoneally in rodents such as rat, guinea pig and the like.
  • These compounds are indicated as inhibitors of autoimmune responses; for example, in tissue or organ transplants where it is desirable to inhibit the host's immune responses.
  • the dosage level is about 100 mg/kg body weight by intramuscular injection.
  • starting compounds of Type II are diazotized to yield compounds of Type Ia.
  • Subsequent alkylation by well known methods yields those compounds of the invention corresponding to structure Ib.
  • Oxidation of Ib with per acids yields the sulfones Id and the reduction of Ib with Raney nickel gives the methylthio derivatives, Ic.
  • the starting materials for Compound II are in turn obtained from the following sources: isatoic anhydrides from Maumee Chemical Co., Toledo, Ohio; dimethylsulfoxide from Crown--Zellerbach Corp., Camas, Washington; NaH from Metal Hydrides, Inc., Beverly, Mass.; ethyl 2-amino-4,5-dimethoxybenzoate was prepared according to Matsmoto, Ber., 11, 135.
  • Part A The preparation of starting material of Type II, Examples 1 through 5.
  • Part B Preparation of final products, Examples 6 through 22.
  • a mixture of 150 ml of dimethylsulfoxide, 350 ml of benzene and 12.7 g (0.3 mole) of 57% sodium hydride-mineral oil dispersion is heated at 70°-75°C for one hour with stirring under nitrogen. The resulting solution is cooled to 30°C.
  • a quantity of 16.3 g (0.1 mole) of isotoic anhydride is added portion-wise over a period of 5 minutes.
  • the temperature rises to 45°C and is kept at 40°-45°C with mild cooling during the addition.
  • the yellow-green solution is allowed to cool over a period of one-half hour when ether is added to two liters volume.
  • the resulting precipitate is filtered off (hygroscopic), washed well with ether, dried somewhat and dissolved in 100 ml of water.
  • the solution is treated with 15 g (0.25 mole) of glacial acetic acid. Decarboxylation is spontaneous with evolution of carbon dioxide. After several minutes, solid potassium carbonate is added to neutralize and then to saturate the solution.
  • the separated oil is extracted into 250 ml of ethyl acetate and the solution is dried (potassium carbonate) filtered and concentrated to give 10.9 g (55.3%) of a solid melting at 100°-102°C.
  • the crude is recrystallized from ethyl acetate to give pure yellow crystals melting at 101°-103°C.
  • This compound was prepared by reacting a solution of 13.2 g of NaH (57%) in a mixture of 180 ml. of DMSO and 360 ml. of benzene with 16.8 g of methyl 4-chlororanthranilate (J.A.C.S. 68 1287 (1946) Lutz, et al.) in analogous fashion to 2'-amino-4',5'-dimethoxy-2-(methylsulfinyl)acetophenone. The material was recrystallized from abs. ethanol, m.p. 129°-32°; yield 15 g (72%).
  • This compound was prepared by reacting a solution of 44 g of NaH (57%) in a mixture of 600 ml. of DMSO and 1200 ml. of benzene with 50 g of methyl 5-methyl anthranilate (J. Med. Chem. 11 500) in analogous fashion to 2'-amino-4',5'-dimethoxy-2-(methylsulfinyl)acetophenone.
  • the material was recrystallized from ethyl acetate with the aid of charcoal, m.p. 145°-47°; yield 30 g (47%).
  • This compound was prepared by diazotizing a solution of 18.5 g of 2'-amino-5'-methyl-2-(methylsulfinyl)acetophenone in 500 ml of 1N HCl with 6.3 g of NaNO 2 in analogous fashion to 6-chloro-3-(methylsulfinyl)-4(1H)-cinnolinone.
  • the material was recrystallized from DMF, m.p. 265°-67°; yield 15 g (77%).
  • the material was recrystallized from CH 3 CN, m.p. 270°-72°; yield 7.5 g (71%).
  • This compound was prepared by reacting a solution of 8 g of 6-methyl-3-methylsulfinyl)-4(1H)-cinnolinone in 145 ml of 1N NaOH with 13.5 g of dimethylsulfate in analogous fashion to 1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone.
  • the material was recrystallized from ethyl acetate, m.p. 173°-75°; yield 5.5 g (65%).

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Abstract

3-substituted cinnolinones having the following structural formula are disclosed: ##SPC1##
Wherein R1 is hydrogen, lower alkyl, aralkyl or acyl and R2 and R3 are hydrogen, halogen, lower alkoxy or lower alkyl, and X is ##EQU1## CH3 COOCH2 S-, or ##SPC2##
These compounds are useful as immunosuppressants.

Description

This is a division of application Ser. No. 190,293 filed Oct. 18, 1971.
The present invention relates to 3-substituted cinnolinones having the following structural formula: ##SPC3##
Wherein R1 is H, lower alkyl, aralkyl or acyl and R2 and R3 are hydrogen, halogen, lower alkoxy or lower alkyl, and X is ##EQU2## ##SPC4## and CH3 COOCH2 S--.
In the above definitions for R1, R2 and R3 the term "lower alkyl" and the "alkyl" portion of lower alkoxy is meant to contain from 1 to 6 carbon atoms such as methyl, ethyl, propyl, isopropyl and the like.
The term "aralkyl" is meant to be those groups such as phenyl lower alkyl, typically benzyl, phenethyl and the like.
The term "acyl" includes lower alkanoic acids from 1 to 6 carbons, typically acetic, propionic, and the like.
The compounds of this invention exhibit potent immuno-suppressant activity in a mammalian host. For example, when they are tested in accordance with the procedure described by Jerne, et al., in "Cell-Bound Antibodies," Page 109, Wistar Institute Press, Philadelphia, Pennsylvania (1963), they are capable of inhibiting 90% of the antibody formation at a dose level of 100 mg/kg intraperitoneally in rodents such as rat, guinea pig and the like.
These compounds are indicated as inhibitors of autoimmune responses; for example, in tissue or organ transplants where it is desirable to inhibit the host's immune responses. The dosage level is about 100 mg/kg body weight by intramuscular injection.
In order to use these compounds they are formulated with pharmaceutically acceptable diluents such as water for injection, sesame oil, and the like, by well known methods to the art into dosage forms suitable for intramuscular injection.
The above compounds are prepared in accordance with the following reaction scheme: ##SPC5##
Broadly speaking, starting compounds of Type II are diazotized to yield compounds of Type Ia. Subsequent alkylation by well known methods yields those compounds of the invention corresponding to structure Ib. Oxidation of Ib with per acids yields the sulfones Id and the reduction of Ib with Raney nickel gives the methylthio derivatives, Ic.
The compounds of the invention corresponding to structures Ia and Ib above undergo Pummerer rearrangement in presence of an acid anhydride to give products of type Ie. ##SPC6##
Compounds of Type Ie, upon refluxing with aqueous mineral acid are converted to compounds of Type If. ##SPC7##
Starting materials of Type II are prepared as follows: ##SPC8##
The starting materials for Compound II are in turn obtained from the following sources: isatoic anhydrides from Maumee Chemical Co., Toledo, Ohio; dimethylsulfoxide from Crown--Zellerbach Corp., Camas, Washington; NaH from Metal Hydrides, Inc., Beverly, Mass.; ethyl 2-amino-4,5-dimethoxybenzoate was prepared according to Matsmoto, Ber., 11, 135.
In order to further illustrate the practice of this invention, the following examples are included:
Part A -- The preparation of starting material of Type II, Examples 1 through 5.
Part B -- Preparation of final products, Examples 6 through 22.
PART A EXAMPLE 1 ##SPC9## 2'-amino-2-(methylsulfinyl)acetophene
Preparation of dimethylsulfoxide anion:
A mixture of 150 ml of dimethylsulfoxide, 350 ml of benzene and 12.7 g (0.3 mole) of 57% sodium hydride-mineral oil dispersion is heated at 70°-75°C for one hour with stirring under nitrogen. The resulting solution is cooled to 30°C.
A quantity of 16.3 g (0.1 mole) of isotoic anhydride is added portion-wise over a period of 5 minutes. The temperature rises to 45°C and is kept at 40°-45°C with mild cooling during the addition. The yellow-green solution is allowed to cool over a period of one-half hour when ether is added to two liters volume. The resulting precipitate is filtered off (hygroscopic), washed well with ether, dried somewhat and dissolved in 100 ml of water. The solution is treated with 15 g (0.25 mole) of glacial acetic acid. Decarboxylation is spontaneous with evolution of carbon dioxide. After several minutes, solid potassium carbonate is added to neutralize and then to saturate the solution. The separated oil is extracted into 250 ml of ethyl acetate and the solution is dried (potassium carbonate) filtered and concentrated to give 10.9 g (55.3%) of a solid melting at 100°-102°C. The crude is recrystallized from ethyl acetate to give pure yellow crystals melting at 101°-103°C.
Anal. Calcd for C9 H11 NO2 S: C, 54.80; H, 5.62; N, 7.10. Found: C, 55.05; H, 5.71; N, 7.15.
EXAMPLE 2 ##SPC10## 2'-amino-4'-chloro-2-(methylsulfinyl)acetophenone
This compound was prepared by reacting a solution of 13.2 g of NaH (57%) in a mixture of 180 ml. of DMSO and 360 ml. of benzene with 16.8 g of methyl 4-chlororanthranilate (J.A.C.S. 68 1287 (1946) Lutz, et al.) in analogous fashion to 2'-amino-4',5'-dimethoxy-2-(methylsulfinyl)acetophenone. The material was recrystallized from abs. ethanol, m.p. 129°-32°; yield 15 g (72%).
Anal. Calcd for C9 H10 ClNO2 S: C, 46.65; H, 4.35; S, 13.84. Found: C, 46.56; H, 4.40; S, 13.87.
EXAMPLE 3 ##SPC11## 2'-amino-5'-chloro-2-(methylsulfinyl)acetophenone
To a mixture of 600 ml. of benzene and 300 ml. of DMSO was added 22 g. of sodium hydride (55% suspension in mineral oil). The mixture was heated at ca. 75° on a water bath under a stream of nitrogen for 1.5 hr., and the clear solution cooled to 25° in an ice bath. The bath was removed and 29.4 g. of 6-chloroisatoic anhydride was added. The temperature rose to 45°. The solution was stirred for 45 minutes and then diluted to ca. 2500 ml. with anhydrous ether. The precipitate was filtered off, washed with anhydrous ether, and dissolved in 175 ml. of H2 O. The solution was treated with 75 ml. of glacial acetic acid, and saturated with K2 CO3. A yellow precipitate formed. This was filtered, washed with cold H2 O, and recrystallized from CH3 CN, mp. 143°-45°; yield 15 g (43%).
Anal. Calcd for C9 H10 ClNO2 S: C, 46.65; H, 4.35; N, 6.05; S, 13.85. Found: C, 46.93; H, 4.35; N, 6.30; S, 13.68.
EXAMPLE 4 ##SPC12## 2'-amino-5'-methyl-2-(methylsulfinyl)acetophenone
This compound was prepared by reacting a solution of 44 g of NaH (57%) in a mixture of 600 ml. of DMSO and 1200 ml. of benzene with 50 g of methyl 5-methyl anthranilate (J. Med. Chem. 11 500) in analogous fashion to 2'-amino-4',5'-dimethoxy-2-(methylsulfinyl)acetophenone. The material was recrystallized from ethyl acetate with the aid of charcoal, m.p. 145°-47°; yield 30 g (47%).
Anal. Calcd for C10 H13 NO2 S: C, 56.85; H, 6.20; N, 6.63; S, 15.18. Found: C, 56.98; H, 6.21; N, 6.49; S, 15.02.
EXAMPLE 5 ##SPC13## 2'-amino-4',5'-dimethoxy-2-(methylsulfinyl)acetophenone
To a mixture of 1 l of benzene and 500 ml of DMSO was added 40 g of NaH (55% in mineral oil). The mixture was heated with stirring at ca. 78° on a water bath under a stream of nitrogen. After 2 hr. hydrogen evolution had ceased, and the solution was clear. The solution was cooled to 25° and 40 g. of ethyl 3,4-dimethoxy anthranilate was added with stirring. The temperature rose to 32°. The mixture was stirred for 45 min. and diluted to 5 l. with anhydrous ether. The precipitated material was filtered, washed with anhydrous ether, and dissolved in 500 ml of H2 O. The aqueous solution was adjusted to ca. pH 6 with glacial acetic acid, and the oil that precipitated was extracted with five 100 ml. portions of chloroform. Comb. extracts were dried over Na2 SO4, and concentrated to a heavy oil under reduced pressure. On cooling the oil crystallized. It was recrystallized from abs. EtOH, mp. 162°-64°; yield 34 g (50%).
Anal. Calcd for C11 H15 NO4 S: C, 51.35; H, 5.88; N, 5.44; S, 12.64. Found: C, 51.54; H, 5.97; N, 5.30; S, 12.63.
EXAMPLE 6 ##SPC14## 6-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone
This compound was prepared by diazotizing a solution of 18.5 g of 2'-amino-5'-methyl-2-(methylsulfinyl)acetophenone in 500 ml of 1N HCl with 6.3 g of NaNO2 in analogous fashion to 6-chloro-3-(methylsulfinyl)-4(1H)-cinnolinone. The material was recrystallized from DMF, m.p. 265°-67°; yield 15 g (77%).
Anal. Calcd for C10 H10 N2 O2 S: C, 54.04; H, 4.54; N, 12.60; S, 14.43. Found: C, 53.82; H, 4.63; N, 12.60; S, 14.56
PART B EXAMPLE 7 ##SPC15## 3-(Methylsulfinyl)-4(1H)-cinnolinone
A solution of 5.0 g (0.025 mole) of 2'-amino-2-(methylsulfinyl)-acetophenone, 30 ml (0.03 mole) of cold (15°C) 1N hydrochloric acid and 100 ml of cold water cooled to 5°C. A solution of 2.07 g (0.03 mole) of sodium nitrite in 10 ml of water was added over a period of 3 minutes with stirring, keeping the temperature at 5°C. A deep red color developed as yellow solid separated. The mixture was allowed to warm up to 20°C. After 15 minutes at 20° the product was filtered, washed with water, 2-propanol and then ether. Wt 5.0 g (64%) mp. 266°-269°. Recrystallization from N,N-dimethylformamide gave pure, white crystals melting at 274°-276°C.
Anal. Calcd. for C9 H8 N2 O2 S: C, 51.91; H, 3.87; N, 13.45. Found: C, 51.89; H, 3.98; N, 13.41.
EXAMPLE 8 ##SPC16## 6-Chloro-3-(methylsulfinyl)-4(1H)-cinnolinone
500 ml of 3N HCl was chilled to 0° in an ice-salt bath, and 10 g of 2'-amino-5'-chloro-2-(methylsulfinyl)acetophenone was added. The mixture was stirred until a clear solution was obtained, and a solution of 3.45 g of NaNO2 in 20 ml of H2 O was added with stirring at ca. 0°-3°. The solution became first orange colored, and then a yellow precipitate formed. The ice bath was removed, and the mixture was stirred until room temperature was attained. The precipitate was filtered off, washed with H2 O, and recrystallized from dimethylformamide, mp. 267°-72°; yield 5 g (44%).
Anal. Calcd. for C9 H7 ClN2 O2 S: C, 44.54; H, 2.91; N, 11.54; S, 13.21. Found: C, 44.62; H, 2.98; N, 11.54; S, 12.96.
EXAMPLE 9 ##SPC17## 7-Chloro-3-(methylsulfinyl)-4(1H)-cinnolinone
This was prepared in analogous fashion to 6-chloro-3-(methylsulfinyl)-4(1H)-cinnolinone by diazotizing a suspension of 11 g of 2'-amino-4'-chloro-2-(methylsulfinyl) acetophenone in 250 ml of 1N HCl with 3.5 g of NaNO2. The material was recrystallized from dimethyl formamide m.p. 285°-90°; yield 10 g (87%).
Anal. Calcd. for C9 H7 ClN2 O2 S: C, 44.54; H, 2.91; N, 11.54. Found: C, 44.38; H, 3.07; N, 11.72.
EXAMPLE 10 ##SPC18## 6,7-Dimethoxy-3-(methylsulfinyl)-4(1H)-cinnolinone
A solution of 20 g of 2'-amino-3',4'-dimethoxy-2-(methylsulfinyl) acetophenone in 250 ml of 1N HCl at 0° was treated dropwise with stirring at 0°-5° with a solution of 5.6 g of NaNO2 in 30 ml of H2 O. The solution became brown, and a peach colored precipitate formed. The mixture was allowed to warm up to room temperature and the precipitate was filtered, washed with cold H2 O, and recrystallized from dimethylformamide, mp. 303°-05°; yield 17 g (81%).
Anal. Calcd. for C11 H12 N2 O4 S: C, 49.25; H, 4.51; N, 10.44; S, 11.95. Found: C, 49.37; H, 4.75; N, 10.56; S, 11.85.
EXAMPLE 11 ##SPC19## 1-Methyl-3-(methylsulfinyl)-4(1H)-cinnolinone
Dimethylsulfate [12.5 g (0.1 mole)] was added gradually to a vigorously stirred solution of 6.5 g (0.0298 mole) of 3-(methylsulfinyl)-4(1H)-cinnolinone in 120 ml of 1N sodium hydroxide solution at 30°C. The temperature rose to 40° as the suspended dimethyl sulfate gradually went into solution over a period of 15 minutes. After an additional one-half hour of stirring, potassium carbonate excess was added to salt-out an oil. The product was extracted into 800 ml of methylene chloride, the solution was dried over K2 CO3, charcoaled, filtered and concentrated. Wt 6.4 g (96.7%) mp. 187°-189°C. Recrystallization from 2-propanol-petroleum ether gave pure material, mp. 189°-191°C.
Anal. Calcd. for C10 H10 N2 O2 S: C, 54.04; H, 4.54; N, 12.60; S, 14.43. Found: C, 54.00; H, 4.55; H, 12.53; S, 14.67.
EXAMPLE 12 ##SPC20## 6-Chloro-1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone
To a solution of 10 g of 6-chloro-3-(methylsulfinyl)-4(1H) cinnolinone in 160 ml of 1N NaOH, was added 15 g of (CH3)2 SO4 with stirring. The temperature rose to ca 36°, and a thick pasty precipitate formed. After the mixture was allowed to stand for 0.5 hr., it was filtered. The solids were washed with H2 O, and recrystallized from abs. ethanol, mp. 231.5°-34.5° yield 6g (60%).
Anal. Calcd. for C10 H9 ClN2 O2 S: C, 46.79; H, 3.53; N, 10.91; S, 12.49. Found: C, 47.04; H, 3.60; N, 11.20; S, 12.49.
EXAMPLE 13 ##SPC21## [(6-Chloro-1,4-dihydro-1-methyl-4-oxo-3-cinnolinyl)thio]methanol acetate.
A mixture of 8 g of 6-chloro-1-methyl-3-(methylsulfinyl)-4(1H) cinnolinone and 30 ml of acetic anhydride was refluxed for 21/2 hrs. The resulting solution was allowed to stand at room temperature overnight. The crystalline precipitate was filtered off, washed with Skelly B, and recrystallized from CH3 CN, mp. 191°-92°; yield 6 g (65%).
Anal. Calcd. for C12 H11 ClN2 O3 S: C, 48.25; H, 3.71; N, 9.38; S, 10.73. Found: C, 48.22; H, 3.67; N, 9.59; S, 10.47.
EXAMPLE 14 ##SPC22## [(1-acetyl-6-chloro-1,4-dihydro-4-oxo-3-cinnolinyl)thio]methanol acetate
A mixture of 12 g of 6-chloro-3-(methylsulfinyl)-4(1H)-cinnolinone and 100 ml of acetic anhydride was refluxed for 3 hours. The solution was chilled, and the crystalline precipitate filtered off, washed with Skelly B, and recrystallized from ethyl acetate, mp. 148°-50°; yield 4 g (24.5%).
Anal. Calcd. for C13 H11 ClN2 O4 S: C, 47.79; H, 3.39; N, 8.57; S, 9.81. Found: C, 48.06; H, 3.54; N, 8.49; S, 10.02.
EXAMPLE 15 ##SPC23## [(1-Acetyl-1,4-dihydro-6,7-dimethoxy-4-oxo-3-cinnolinyl)thio]methanol acetate
A mixture of 13 g of 6,7-dimethoxy-3-(methylsulfinyl)-4(1H) cinnolinone and 500 ml of acetic anhydride was refluxed for 3 hours. The resulting solution was chilled, and the precipitate was filtered off, washed with Skelly B, and recrystallized from CH3 CN, mp. 208°-209.5°; yield 11 g (63%).
Anal. Calcd. for C15 H16 N2 O6 S: C, 51.13; H, 4.58; N, 7.95; S, 9.10. Found: C, 51.25; H, 4.65; N, 8.12; S, 9.28.
EXAMPLE 16 ##SPC24## 6,7-Dimethoxy-1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone
A solution of 10 g of 6,7-dimethoxy-3-(methylsulfinyl)-4(1H)-cinnolinone in 148 ml of 1 normal NaOH was treated with 14 g of (CH3)2 SO4 with stirring. As the (CH3)2 SO4 dissolved, the temperature rose to ca. 35° and a pasty precipitate formed. The mixture was stirred for 45 minutes and the precipitate was filtered off, washed with cold H2 O and recrystallized from CH3 CN, mp. 262°-64°; yield 6 g (57%).
Anal. Calcd. for C12 H14 N2 O4 S: C, 51.05; H, 5.00; N, 9.92; S, 11.36. Found: C, 51.32; H, 5.24; N, 10.13; S, 11.53.
EXAMPLE 17 ##SPC25## [(1,4-Dihydro-6,7-dimethoxy-1-methyl-4-oxo-3-cinnolinyl)thio]methanol acetate
A mixture of 11 g of 6,7-dimethoxy-1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone and 100 ml of acetic anhydride was refluxed for 2 hours. The solution was chilled, and the crystalline precipitate was filtered off, washed with Skelly B, and recrystallized from CH3 CN, mp. 229°-33°, yield 11 g (87%).
Anal. Calcd. for C14 H16 N2 O5 S: C, 51.84; H, 4.97; N, 8.64; S, 9.89. Found: C, 51.86; H, 5.09; N, 8.41. S, 10.03.
EXAMPLE 18 ##SPC26## 3,3'-Methylenedithiobis(6-chloro-1-methyl-4(1H)-cinnolinone)
A mixture of 10 g of [(6-chloro-1,4-dihydro-1-methyl-4-oxo-3-cinnolinyl)-thio]methanol acetate and 250 ml of 3N HCL was refluxed with stirring for 5 hours. The mixture was then chilled, and the precipitate filtered off washed with cold H2 O, and recrystallized from dimethylformamide, mp. 352°-54°; yield 5.5 g (73%).
Anal. Calcd. for C19 H14 Cl2 N4 O2 S2 : C, 49.04; H, 3.03; N, 12.04; S, 13.78. Found: C, 49.23; H, 3.22; N, 12.24; S, 13.60.
EXAMPLE 19 ##SPC27## 1-Methyl-3-(methylthio)-4(1H)-cinnolinone
A mixture of 0.4 g (0.0018 mole) of 1-methylsulfinyl)-4(1H)-cinnoline, 50 ml of water and 3.5 g of Raney nickel was boiled with stirring for 10 minutes. The cooled reaction mixture was filtered. The Raney nickel was extracted with 50 ml of methylene chloride. The dried (K2 CO3) extract concentrated to give 10 mg (2.7%) of yellow crystals melting at 173°-175°. Recrystallization from benzene-petroleum ether gave pure material, m.p. 175°-177°C.
Anal. Calcd. for C10 H10 N2 OS: C, 58.23; H, 4.89; N, 13.58. Found: C, 58.44; H, 4.90; N, 13.64.
EXAMPLE 20 ##SPC28## 1-Methyl-3-(methylsulfonyl)-4(1H)-cinnolinone
A quantity of 6.16 g (0.027 mole) of 85% m-chloroperbenzoic acid was added to a solution of 6.6 g (0.03 mole) of 1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone in 100 ml of chloroform. The temperature rose to 45° C. After 5 minutes the solution was brought to reflux for 5 minutes, cooled, mixed with 200 ml of 5% sodium bicarbonate and stirred for 10 minutes. Additional chloroform (300 ml) was added to dissolve the separated product. The organic layer was separated, dried over anhydrous potassium carbonate and concentrated to give 6.7 g (94.4%) of white product melting at 202°-204°. Recrystallization from chloroform-methanol gave pure product melting at 204°-206° C.
Anal. Calcd. for C10 H10 N2 O3 S: C, 50.41; H, 4.23; N, 11.76. Found: C, 50.46; H, 4.30; N, 11.80.
EXAMPLE 21 ##SPC29## 7-Chloro-1-methyl-3-(methylsulfonyl)-4(1H)-cinnolinone
This was prepared by oxidizing a solution of 10 g of 7-chloro-1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone in 500 ml of CHCl3 with 7.5 g of m-chloroperbenzoic acid in analogous fashion to 1-methyl-3-(methylsulfonyl)-4(1H)-cinnolinone. The material was recrystallized from CH3 CN, m.p. 270°-72°; yield 7.5 g (71%).
Anal. Calcd. for C10 H9 ClN2 O3 S: C, 44.04; H, 3.33; N, 10.27; S, 11.76. Found: C, 44.32; H, 3.22; N, 10.29; S, 12.05.
EXAMPLE 22 ##SPC30## 1,6-dimethyl-3-(methylsulfinyl)-4(1H)-cinnolinone
This compound was prepared by reacting a solution of 8 g of 6-methyl-3-methylsulfinyl)-4(1H)-cinnolinone in 145 ml of 1N NaOH with 13.5 g of dimethylsulfate in analogous fashion to 1-methyl-3-(methylsulfinyl)-4(1H)-cinnolinone. The material was recrystallized from ethyl acetate, m.p. 173°-75°; yield 5.5 g (65%).
Anal. Calcd for C11 H12 N2 O2 S: C, 55.91; H, 5.12; W, 11.86; S, 13.57. Found: C, 56.19; H, 5.17; N, 11.97; S, 13.71.

Claims (1)

We claim:
1. A process for the production of a compound of formula I: ##SPC31##
wherein R1 is methyl, and R2 and R3 are hydrogen, chlorine, methyl and methoxy, comprising the steps of:
a. treating compounds of formula II: ##SPC32##
with sodium nitrite and hydrochloric acid to give a compound of formula III: ##SPC33##
wherein R2 and R3 are as hereinbefore defined;
b. treating compounds of formula III wherein R2 and R3 are as hereinbefore defined with a dialkylsulfate having 1 to 6 carbon atoms in the alkyl residue and an alkali metal hydroxide; and
c. recovering the products of formula I wherein R1, R2 and R3 are as hereinbefore defined.
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US4192873A (en) * 1976-11-25 1980-03-11 Ciba-Geigy Corporation Anti-inflammatory 2-sulphonyl- (or -sulphinyl)-2'-aminoacetophenones
US4956460A (en) * 1987-04-23 1990-09-11 Industria Chimica Profarmaco S.P.A. Process for the preparation of 1-alkyl-3-carboxy-4-cinnolones
FR2683221A1 (en) * 1991-11-04 1993-05-07 Pf Medicament NOVEL CINNOLINONES-4 DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE.

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4192873A (en) * 1976-11-25 1980-03-11 Ciba-Geigy Corporation Anti-inflammatory 2-sulphonyl- (or -sulphinyl)-2'-aminoacetophenones
US4263455A (en) * 1976-11-25 1981-04-21 Ciba-Geigy Corporation Novel 2-sulphonyl- (or -sulphinyl)-2'-aminoacetophenones
US4956460A (en) * 1987-04-23 1990-09-11 Industria Chimica Profarmaco S.P.A. Process for the preparation of 1-alkyl-3-carboxy-4-cinnolones
FR2683221A1 (en) * 1991-11-04 1993-05-07 Pf Medicament NOVEL CINNOLINONES-4 DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE.
WO1993009098A1 (en) * 1991-11-04 1993-05-13 Pierre Fabre Medicament Novel 4-cinnolinone derivatives, their preparation and application in therapy

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